Methods, compositions, and delivery systems for therapeutic skin treatments
US-2024390236-A1 · Nov 28, 2024 · US
US2016303034A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016303034-A1 |
| Application number | US-201615099991-A |
| Country | US |
| Kind code | A1 |
| Filing date | Apr 15, 2016 |
| Priority date | Apr 16, 2015 |
| Publication date | Oct 20, 2016 |
| Grant date | — |
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Ampoule containing a Pro-Resolution Pathway Stimulator, methods for making, and treating for skin having discrete areas of inflammation using ampoule composition containing Pro-Resolution Pathway Stimulator.
Opening claim text (preview).
1 . A unit dose package containing a composition comprising at least one Pro-Resolution Pathway Stimulator. 2 . The unit dose package of claim 1 which is a capsule or a facial treatment mask. 3 . The unit dose package of claim 2 where the capsule is an ampoule. 4 . The unit dose package of claim 1 where the Pro-Resolution Pathway Stimulator is an Inflammatory Metabolite Inhibitor, a Pro-Resolving Activator, or mixtures thereof. 5 . The unit dose package of claim 4 wherein the Pro-Resolution Pathway Stimulator is a Pro-Resolving Activator. 6 . The unit dose package of claim 4 wherein the Pro-Resolution Pathway Stimulator is both an Inflammatory Metabolite Inhibitor and a Pro-Resolving Activator. 7 . The unit dose package of claim 2 wherein the capsule is made of gelatin. 8 . The unit dose package of claim 7 wherein the gelatin is a plant derived gelatin. 9 . The unit dose package of claim 8 wherein the plant derived gelatin is a hydrocolloid selected from carrageenan, seaweed, or mixtures thereof. 10 . The unit dose package of claim 8 wherein the gelatin comprises 1-25% gelatin, 1-60% starch, and 1-30% plasticizer. 11 . A method for making a unit dose package containing a composition comprising at least one Pro-Resolution Pathway Stimulator comprising the steps of: (a) selecting an active ingredient; (b) quantifying: (i) the inhibition in release of one or more Inflammatory Metabolites or Inflammatory Metabolite Markers from cells to which the active is exposed, and/or (ii) the increase in release of one or more Pro-Resolving Lipid Mediators or Pro-Resolving Lipid Mediator Markers in cells exposed to the active, (c) selecting the active that shows: (i) a decrease in release of Inflammatory Metabolites or Inflammatory Metabolite Markers individually or in combination; and/or (ii) an increase in release of Pro-Resolving Lipid Mediators or Pro-Resolving Lipid Mediator Markers individually or in combination (d) formulating the active selected in (c) into a composition; and (e) packaging the composition of (e) into a unit dose package. 11 . The method of claim 11 where the unit dose package is a capsule. 12 . The method of claim 11 where the capsule is an ampoule. 13 . The method of claim 12 wherein the Pro-Resolution Pathway Stimulator is an Inflammatory Metabolite Inhibitor, a Pro-Resolving Activator or both. 14 . The method of claim 12 wherein the ampoule is made of gelatin. 15 . The method of claim 14 wherein the gelatin is derived from plants. 16 . The method of claim 15 wherein the gelatin is a hydrocolloid which is carrageenan, seaweed, or mixtures thereof. 17 . The method of claim 13 wherein the Pro-Resolution Pathway Stimulator is an Inflammatory Metabolite Inhibitor that causes a decrease in cellular concentration of Inflammatory Metabolites. 18 . The method of claim 13 wherein the Pro-Resolution Pathway Stimulator is a Pro-Resolving Activator. 19 . The method of claim 18 wherein the Pro-Resolving Activator stimulates an increase in cellular concentration of Pro-Resolution Lipid Mediators. 20 . The method of claim 19 wherein the Pro-Resolution Lipid Mediators are Resolvin, Protectin, Lipoxin, or Maresin. 21 . A method for treating skin that has discrete areas of inflammation or to inhibit skin inflammation by: (a) formulating a composition containing at least one Pro-Resolution Pathway Stimulator, (b) packaging the composition into a package, (c) applying the contents of the package to the discrete areas of inflammation on the skin in need of such treatment. 22 . The method of claim 21 wherein the skin is treated with a skin care product prior to treating the discrete areas of inflammation on the skin. 23 . The method of claim 21 wherein the discrete areas of inflammation on the skin are first treated with the ampoule composition followed by application of a skin cream or lotion to the entire skin surface.
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